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trisomy
三染色体细胞
常用释义
英音[ ˈtraɪsəʊmi ]
美音[ ˈtraɪsoʊmi ]
基本释义
  • n. 三染色体细胞;三染色体性
例句
  • 1·If this is a patient with trisomy 21, it become more complicated.
    如果这病人是21三体,可能就复杂些。
  • 2·In this paper, we report a case of X-trisomy, and analyse its mechanism and genetic effect.
    本文报告一例单纯性x三体型,并对其发病机理和遗传效应进行了分析。
  • 3·Down syndrome (trisomy 21) is a disorder caused by the presence of an extra 21st chromosome.
    唐氏综合症(21三体综合症)是由于患者额外多了一条21号染色体所致的疾病。
  • 4·Objective:To evaluate sonographic characteristics on prenatal ultrasound study of trisomy 13 and 18…
    目的:对13及18三体综合征胎儿的超声表现特征和产前超声筛查价值的评价。
  • 5·Trisomy has been the focus of extensive medical research but the exact mechanism is still not understood.
    三体综合症在医学研究上备受关注,但其确切机制仍未明确。
  • 6·This confirmed the presence of tetrasomy 8 and trisomy 8 and also revealed a low percentage of a pentasomy 8 clone.
    这不但证实了三体8和四体8克隆的存在,还发现存在一个较小的五体8克隆。
  • 7·The abnormal is concerned in trisomy, monosomy, Robertsonian translocation, reciprocal translocation and rearrange.
    异常核型涉及到三体型、单体型、罗伯逊易位、相互易位、不平衡重排等。
  • 8·An aneuploid state in which a third homologous chromosome is present in addition to the normal autosomal pair is called trisomy.
    除了正常染色体对以外,还存在有第二种同源染色体的非整倍体状态,被称为三体性。
  • 9·Results: The trisomy with cleft palate mouse foetuses had significantly developmental hypoplasia in the primary palatal shelves.
    结果:该模型虽无原发腭裂却伴有原发腭的发育不足;
  • 10·Results Nine cases of trisomy 18 and 2 cases of other abnormal karyotype were found among the 128 pregnant women (8.59%, 11/128).
    结果128例胎儿核型中,9例为18三体综合征,2例为其它染色体异常,染色体异常发现率为8·59%(11/128)。